RILUZOLE

Product NDC

68084-908

11-digit product format

680840908

Labeler code

68084

Product ID

68084-908_99820b99-6473-998b-e053-2995a90a7fb5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RILUZOLE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA091300

Marketing category

ANDA

Marketing start

2015-03-31

Marketing end

2020-10-31

Substance

RILUZOLE

Active strength

50 mg/1

Pharmacologic classes

Benzothiazole [EPC],Benzothiazoles [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record